Skip to main content
OpenTrials
Completed

NCT Number: NCT03687346

Biological Risk Factors for Onset of Binge Eating and Compensatory Behaviors

The purpose of this proposed project is to test whether several biological factors (such as elevated brain reward region and attention region response to high-calorie foods, weaker inhibitory region response to high-calorie foods, habitual caloric deprivation, and elevated limbic region responsivity) increase the risk of problematic eating (bingeing and purging) in female adolescents.

Completed

Looking for future studies?

Notify Me

Key information

Age range

13 year–16 year

Sex eligibility

Female

Study type

Observational

Primary location

Oregon Research Institute

Eugene, Oregon, 97403, United States

About this study

Participants will be adolescent girls aged 13-16, some of whom will have parental history of eating pathology. Participants will be recruited from the general population but their age, gender, and the presence of parental lifetime eating pathology will create a high-risk sample. The goals of the proposed project are to (1) conduct a prospective high-risk study to test whether proposed biological risk factors predict the future onset of core ED symptoms (e.g., binge eating, compensatory behaviors); (2) test hypotheses regarding how these biological risk factors and established self-report ED risk factors may work together to predict ED behavior onset; (3) examine if certain biological factors account for the effects of certain established self-reported ED risk factors (e.g., elevated brain response to thin models accounts for the effect of questionnaire-measured thin-ideal internalization). The participants will complete a baseline assessment and then follow-ups assessments over a span of three years. In addition, participants will complete one fMRI scan after the first assessment.

During the COVID-19 shelter-at-home order, the investigators will not measure in person only outcomes including fMRI scans, height and weight measurement for BMI calculation nor IAT computer paradigms for all participants that have assessments due during this order.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

  • Inclusion Criteria:
  • Female
  • Aged 13-16 years
  • Exclusion Criteria:
  • Adolescents who report functional magnetic resonance imaging (fMRI) contraindications
  • Current Diagnostic and Statistical Manual of Mental Disorders 5 (DSM-5) substance abuse disorder, eating disorder (ED), conduct disorder, attention deficit hyperactivity disorder (ADHD), or bipolar disorder
  • Weekly or greater use of psychoactive drugs (e.g., analgesics, cocaine, marijuana)
  • Serious medical complications (e.g., cancer, diabetes)
  • History of head injury
  • Relevant food allergies
  • BMI > 35

Treatment and study plan

Primary outcomes

  1. Change in binge eating behaviors using the EDDI

    Time frame: 6 months, 1 year, 2 year, and 3 year follow-up

    Eating Disorder Diagnostic Interview (EDDI)

  2. Change in compensatory behaviors using the EDDI

    Time frame: 6 months, 1 year, 2 year, and 3 year follow-up

    Eating Disorder Diagnostic Interview (EDDI)

Sponsors and collaborators

Lead sponsor

Oregon Research Institute

Other

Registry information

Important dates

Study start
2017
Primary completion
2021
Study completion
2021
First posted
Sep 27, 2018
Registry last updated
Nov 3, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.